Evidence map›Paper›PMID 27206795›Full record

ArticleOncotarget2016

Tumor-selective replication herpes simplex virus-based technology significantly improves clinical detection and prognostication of viable circulating tumor cells.

Wen Zhang, Li Bao, Shaoxing Yang, Zhaoyang Qian, Mei Dong, Liyuan Yin, Qian Zhao, Keli Ge, Zhenling Deng, Jing Zhang and 25 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
2.7field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 2 syntheses or guidelines pooled it, 47 citations in OpenAlex.

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  11. HSV: The scout and assault for digestive system tumors.Frontiers in molecular biosciences · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

35 authors at 12 institutions in 2 countries.

Wen ZhangDepartment of Immunology, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Li BaoBGI-Shenzhen, Shenzhen 518083, China.
Shaoxing YangDepartment of Pulmonary Oncology, Affiliated Hospital, Academy of Military Medical Science, Beijing 100071, China.
Zhaoyang QianBGI-Shenzhen, Shenzhen 518083, China.
Mei DongDepartment of Medical Oncology, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Liyuan YinState Key Laboratory of Molecular Oncology, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Qian ZhaoDepartment of Pathology, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Keli GeDepartment of Immunology, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Zhenling DengDepartment of Immunology, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Jing ZhangDepartment of Medical Oncology, Cancer Center, West China Hospital of Sichuan University, Chengdu 610041, China.
Fei QiDepartment of Respiratory Diseases, Chinese PLA General Hospital, Beijing 100853, China.
Zhongxue AnBGI-Shenzhen, Shenzhen 518083, China.
Yuan YuBGI-Shenzhen, Shenzhen 518083, China.
Qingbo WangBGI-Shenzhen, Shenzhen 518083, China.
Renhua WuBGI-Shenzhen, Shenzhen 518083, China.
Fan FanBGI-Shenzhen, Shenzhen 518083, China.
Lianfeng ZhangInstitute of Laboratory Animal Science, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 10021, China.
Xiping ChenInstitute of Environmental Health and Related Product Safety, China CDC, Beijing 10021, China.
Yingjian NaInstitute of Environmental Health and Related Product Safety, China CDC, Beijing 10021, China.
Lin FengState Key Laboratory of Molecular Oncology, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Lingling LiuDepartment of Immunology, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Yujie ZhuDepartment of Immunology, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Tiancheng QinState Key Laboratory of Molecular Oncology, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Shuren ZhangDepartment of Immunology, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Youhui ZhangDepartment of Immunology, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Xiuqing ZhangBGI-Shenzhen, Shenzhen 518083, China.
Jian WangBGI-Shenzhen, Shenzhen 518083, China.
Xin YiBGI-Shenzhen, Shenzhen 518083, China.
Liqun ZouDepartment of Medical Oncology, Cancer Center, West China Hospital of Sichuan University, Chengdu 610041, China.
Hong-Wu XinLaborartory of Molecular Oncology, Key Laboratory of Carcinogenesis and Translational Research, Ministry of Education, Peking University Cancer Hospital and Institute, Beijing 100142, China.
Henrik J DitzelDepartment of Cancer and Inflammation Research, Institute of Molecular Medicine, University of Southern Denmark, DK-5000 Odense C, Denmark.
Hongjun GaoDepartment of Pulmonary Oncology, Affiliated Hospital, Academy of Military Medical Science, Beijing 100071, China.
Kaitai ZhangState Key Laboratory of Molecular Oncology, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Binlei LiuHubei Provincial Cooperative, Innovation Center of Industrial Fermentation, Hubei University of Technology, Wuhan 30068, China.
Shujun ChengState Key Laboratory of Molecular Oncology, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Chinese Academy of Medical Sciences & Peking Union Medical College · CNBGI Group (China) · CNAcademy of Military Medical Sciences · CNWest China Hospital of Sichuan University · CNChina National Center for Food Safety Risk Assessment · CNChinese Center For Disease Control and Prevention · CNChinese PLA General Hospital · CNInstitute of Laboratory Animal Science · CNOdense University Hospital · DKPeking University · CNSichuan University · CNUniversity of Southern Denmark · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Detection of circulating tumor cells remains a significant challenge due to their vast physical and biological heterogeneity. We developed a cell-surface-marker-independent technology based on telomerase-specific, replication-selective oncolytic herpes-simplex-virus-1 that targets telomerase-reverse-transcriptase-positive cancer cells and expresses green-fluorescent-protein that identifies viable CTCs from a broad spectrum of malignancies. Our method recovered 75.5-87.2% of tumor cells spiked into healthy donor blood, as validated by different methods, including single cell sequencing. CTCs were detected in 59-100% of 326 blood samples from patients with 6 different solid organ carcinomas and lymphomas. Significantly, CTC-positive rates increased remarkably with tumor progression from N0M0, N+M0 to M1 in each of 5 tested cancers (lung, colon, liver, gastric and pancreatic cancer, and glioma). Among 21 non-small cell lung cancer cases in which CTC values were consecutively monitored, 81% showed treatment-related decreases, which was also found after treatments in the other solid tumors. Moreover, monitoring CTC values provided an efficient treatment response indicator in hematological malignancies. Compared to CellSearch, our method detected significantly higher positive rates in 40 NSCLC in all stages, including N0M0, N+M0 and M1, and was less affected by chemotherapy. This simple, robust and clinically-applicable technology detects viable CTCs from solid and hematopoietic malignancies in early to late stages, and significantly improves clinical detection and treatment prognostication.

Indexed as

Neoplastic Cells, CirculatingSimplexvirusAdultAgedBiomarkers, TumorBrain NeoplasmsCarcinoma, Non-Small-Cell LungCase-Control StudiesCell CountCell MembraneCell SeparationDisease ProgressionEpitheliumFemaleFlow CytometryGreen Fluorescent ProteinsBiomarkers, TumorGreen Fluorescent ProteinsTelomeraseclinical applicationepithelial-marker-independenttelomerase-specific HSVviable circulating tumor cells

Identifiers

PMID27206795
PMCPMC5129969
OpenAlexW2401287670

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.